A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237652



Internal ID20804692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90643260..90643681hg38UCSC Ensembl
chr14:91109604..91110025hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576874
Supporting Variants
Samples
Known GenesTTC7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237652
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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